(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butyldimethylsilyl)oxy)butanoic acid
95%
- Product Code: 87171
CAS:
1333332-17-4
| Molecular Weight: | 455.62 g./mol | Molecular Formula: | C₂₅H₃₃NO₅Si |
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| EC Number: | MDL Number: | MFCD30529785 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butyldimethylsilyl (TBDMS) group protects the hydroxyl group, ensuring selective reactivity during the synthesis process. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology, enabling the development of therapeutic peptides, hormones, and other biologically active molecules. The compound’s protective groups are removed under specific conditions, allowing for precise control over peptide chain assembly.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $69.16 |
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| 1.000 | 10-20 days | $161.38 |
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| 5.000 | 10-20 days | $579.51 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butyldimethylsilyl)oxy)butanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butyldimethylsilyl (TBDMS) group protects the hydroxyl group, ensuring selective reactivity during the synthesis process. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology, enabling the development of therapeutic peptides, hormones, and other biologically active molecules. The compound’s protective groups are removed under specific conditions, allowing for precise control over peptide chain assembly.
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| Stable in pH range | - |
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